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Longitudinal Assessment of Retinal Structure in Achromatopsia Patients With Long-Term Follow-up

PURPOSE: To longitudinally characterize structural retinal changes in achromatopsia (ACHM) over extended follow-up. METHODS: Fifty molecularly confirmed ACHM subjects underwent serial spectral-domain optical coherence tomography (SD-OCT) and fundus autofluorescence (FAF) imaging. Foveal structure on...

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Autores principales: Hirji, Nashila, Georgiou, Michalis, Kalitzeos, Angelos, Bainbridge, James W., Kumaran, Neruban, Aboshiha, Jonathan, Carroll, Joseph, Michaelides, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280917/
https://www.ncbi.nlm.nih.gov/pubmed/30513534
http://dx.doi.org/10.1167/iovs.18-25452
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author Hirji, Nashila
Georgiou, Michalis
Kalitzeos, Angelos
Bainbridge, James W.
Kumaran, Neruban
Aboshiha, Jonathan
Carroll, Joseph
Michaelides, Michel
author_facet Hirji, Nashila
Georgiou, Michalis
Kalitzeos, Angelos
Bainbridge, James W.
Kumaran, Neruban
Aboshiha, Jonathan
Carroll, Joseph
Michaelides, Michel
author_sort Hirji, Nashila
collection PubMed
description PURPOSE: To longitudinally characterize structural retinal changes in achromatopsia (ACHM) over extended follow-up. METHODS: Fifty molecularly confirmed ACHM subjects underwent serial spectral-domain optical coherence tomography (SD-OCT) and fundus autofluorescence (FAF) imaging. Foveal structure on SD-OCT was graded and compared for evidence of progression, and foveal total retinal thickness (FTRT) and outer nuclear layer (ONL) thickness were serially measured. FAF patterns were characterized and compared over time. RESULTS: Mean SD-OCT follow-up was 61.6 months (age range at baseline, 6–52 years). Forty-five of the subjects had serial FAF (mean follow-up: 48.5 months). Only 6 (12%) of the subjects demonstrated qualitative change on serial foveal SD-OCT scans. Among the entire cohort, there was no statistically significant change over time in FTRT (P = 0.2459) or hyporeflective zone (HRZ) diameter (P = 0.3737). There was a small—but statistically significant—increase in ONL thickness (P = 0.0084). Three different FAF patterns were observed: centrally increased FAF (13/45), normal FAF (14/45), and well-demarcated reduced FAF (18/45), with the latter group displaying a small gradual increase in the area of reduced FAF of 0.055 mm(2) over 43.4 months (P = 0.0011). CONCLUSIONS: This longitudinal study of retinal structure in ACHM represents the largest cohort and longest follow-up period to date. Our findings support the presiding notion that ACHM is essentially a stationary condition regarding retinal structure, and any change over time is likely to be small, slow, and variable across patients. This may potentially afford a wider window for therapeutic intervention.
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spelling pubmed-62809172018-12-06 Longitudinal Assessment of Retinal Structure in Achromatopsia Patients With Long-Term Follow-up Hirji, Nashila Georgiou, Michalis Kalitzeos, Angelos Bainbridge, James W. Kumaran, Neruban Aboshiha, Jonathan Carroll, Joseph Michaelides, Michel Invest Ophthalmol Vis Sci Genetics PURPOSE: To longitudinally characterize structural retinal changes in achromatopsia (ACHM) over extended follow-up. METHODS: Fifty molecularly confirmed ACHM subjects underwent serial spectral-domain optical coherence tomography (SD-OCT) and fundus autofluorescence (FAF) imaging. Foveal structure on SD-OCT was graded and compared for evidence of progression, and foveal total retinal thickness (FTRT) and outer nuclear layer (ONL) thickness were serially measured. FAF patterns were characterized and compared over time. RESULTS: Mean SD-OCT follow-up was 61.6 months (age range at baseline, 6–52 years). Forty-five of the subjects had serial FAF (mean follow-up: 48.5 months). Only 6 (12%) of the subjects demonstrated qualitative change on serial foveal SD-OCT scans. Among the entire cohort, there was no statistically significant change over time in FTRT (P = 0.2459) or hyporeflective zone (HRZ) diameter (P = 0.3737). There was a small—but statistically significant—increase in ONL thickness (P = 0.0084). Three different FAF patterns were observed: centrally increased FAF (13/45), normal FAF (14/45), and well-demarcated reduced FAF (18/45), with the latter group displaying a small gradual increase in the area of reduced FAF of 0.055 mm(2) over 43.4 months (P = 0.0011). CONCLUSIONS: This longitudinal study of retinal structure in ACHM represents the largest cohort and longest follow-up period to date. Our findings support the presiding notion that ACHM is essentially a stationary condition regarding retinal structure, and any change over time is likely to be small, slow, and variable across patients. This may potentially afford a wider window for therapeutic intervention. The Association for Research in Vision and Ophthalmology 2018-12 /pmc/articles/PMC6280917/ /pubmed/30513534 http://dx.doi.org/10.1167/iovs.18-25452 Text en Copyright 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Genetics
Hirji, Nashila
Georgiou, Michalis
Kalitzeos, Angelos
Bainbridge, James W.
Kumaran, Neruban
Aboshiha, Jonathan
Carroll, Joseph
Michaelides, Michel
Longitudinal Assessment of Retinal Structure in Achromatopsia Patients With Long-Term Follow-up
title Longitudinal Assessment of Retinal Structure in Achromatopsia Patients With Long-Term Follow-up
title_full Longitudinal Assessment of Retinal Structure in Achromatopsia Patients With Long-Term Follow-up
title_fullStr Longitudinal Assessment of Retinal Structure in Achromatopsia Patients With Long-Term Follow-up
title_full_unstemmed Longitudinal Assessment of Retinal Structure in Achromatopsia Patients With Long-Term Follow-up
title_short Longitudinal Assessment of Retinal Structure in Achromatopsia Patients With Long-Term Follow-up
title_sort longitudinal assessment of retinal structure in achromatopsia patients with long-term follow-up
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280917/
https://www.ncbi.nlm.nih.gov/pubmed/30513534
http://dx.doi.org/10.1167/iovs.18-25452
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